[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100644492":3},{"organization":4,"armGroups":7,"interventions":14,"overallOfficials":19,"centralContacts":19,"locations":20,"responsibleParty":41,"collaborators":43,"id":48,"slug":49,"hasResults":50,"nctId":51,"briefTitle":52,"officialTitle":53,"acronym":54,"eligibilityCriteria":55,"healthyVolunteers":50,"sex":56,"minAge":57,"maxAge":19,"enrollmentInfo":58,"targetDuration":19,"studyType":61,"phases":62,"briefSummary":64,"conditions":65,"keywords":67,"overallStatus":23,"whyStopped":19,"lastUpdateSubmitDate":71,"lastUpdatePostDateStruct":72,"startDateStruct":75,"completionDateStruct":77,"leadSponsor":79,"locationsCount":80},{"fullName":5,"class":6},"Scuola Superiore di Studi Universitari e di Perfezionamento Sant'Anna","OTHER",[8],{"label":9,"type":10,"description":11,"interventionNames":12},"Exo-Assisted","EXPERIMENTAL","Patients perform gait training on treadmill and overground with assistance of the investigational device",[13],"Device: Exo-Assisted",[15],{"type":16,"name":9,"description":17,"armGroupLabels":18,"otherNames":19},"DEVICE","Participants perform gait training assiste by the knee exoskeletn investigational device",[9],null,[21],{"facility":22,"status":23,"city":24,"state":25,"zip":26,"country":27,"countryCode":28,"cosmosGeoPoint":29,"geoPoint":34,"contacts":35},"Don Gnocchi - Centro \"S. Maria della Provvidenza\"","RECRUITING","Roma","RM","00166","Italy","IT",{"type":30,"coordinates":31},"Point",[32,33],11.10642,44.99364,{"lat":33,"lon":32},[36],{"name":37,"role":38,"phone":39,"phoneExt":19,"email":40},"Principal Investigator","CONTACT","+39 0633086500","iaprile@dongnocchi.it",{"type":42,"investigatorFullName":19,"investigatorTitle":19,"investigatorAffiliation":19,"oldNameTitle":19,"oldOrganization":19},"SPONSOR",[44,46],{"name":45,"class":6},"Istituti Clinici Scientifici Maugeri SpA",{"name":47,"class":6},"Fondazione Don Carlo Gnocchi Onlus","100644492","funcitonality-and-safety-of-a-knee-device-for-gait-rehabilitation-in-neurological-patients-100644492",false,"NCT07670325","Funcitonality and Safety of a Knee Device for Gait Rehabilitation in Neurological Patients","Funzionalità e Sicurezza di un Dispositivo di Ginocchio Per Riabilitazione Della Deambulazione Con Pazienti Neurologici","AKO-R","Inclusion Criteria:\n\n* diagnosed stroke with fMRI\n* within 2 years from stroke event\n* FAC\\>= 3\n* height \\[1.5 - 2\\]m\n* weigth \\\u003C= 100 Kg\n\nExclusion Criteria:\n\n* MoCA\\\u003C18\n* Pregnancy\n* Implanted cardiac devices, such as pacemakers or implantable cardioverter defibrillators (ICDs)\n* Recent or current participation in research studies that, in the opinion of the Principal Investigator, may affect the subject's response to the study intervention\n* Severe aphasia\n* MAS=4","ALL","18 Years",{"count":59,"type":60},20,"ESTIMATED","INTERVENTIONAL",[63],"NA","This clinical investigation aims to evaluate the safety, feasibility, and preliminary performance of the AKO-R wearable robotic device for knee assistance during walking. The study involves participants performing treadmill and overground gait training under supervised conditions, with the device providing assistive torque to support movement. Clinical and functional outcomes are assessed using validated measurement tools, while additional data are collected to characterize user performance and interaction with the device. The study is designed as an exploratory investigation to gather evidence supporting the clinical use and further development of the device. Primary outcomes regards safety of the device and preliminary clinical benefit on gait symmetry.",[66],"Stroke",[68,69,70],"exoskeleton","robotics rehabilitation","stroke","2026-06-24",{"date":73,"type":74},"2026-06-26","ACTUAL",{"date":76,"type":74},"2026-06-22",{"date":78,"type":60},"2026-11-30",{"name":5,"class":6},1]